A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13927809



Internal ID6306296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106549300..106551566hg38UCSC Ensembl
Innerchr10:106549331..106551536hg38UCSC Ensembl
Outerchr10:106549270..106551597hg38UCSC Ensembl
chr10:108309058..108311324hg19UCSC Ensembl
Innerchr10:108309089..108311294hg19UCSC Ensembl
Outerchr10:108309028..108311355hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382267
hg192267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624473
Supporting Variants
SamplesNA19909
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13927809
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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